Laporan Praktik Kerja Profesi Apoteker Farmasi Industri di PT. Abbott Indonesia Cimanggis Plant, Depok

Abstract

Objective: This Professional Pharmacist Work Practice (PKPA) is conducted with the aim of enabling prospective pharmacists to understand the roles, functions, and responsibilities of pharmacists as responsible pharmacists in the pharmaceutical industry in accordance with good manufacturing practices (GMP) guidelines and aspects of GMP so that the quality of medicines is maintained until they reach consumers. Method: The Industrial Pharmacy Professional Work Practice (PKPA) at PT. Abbott Indonesia was conducted from May 5 to June 26, 2025. Activities were carried out at PT. Abbott Indonesia in the Quality Assurance department of the Quality Document Control & Regulatory Compliance (QDoc) division, and participants gained knowledge about other departments at PT. Abbott Indonesia. Results: Quality assurance at PT. Abbott Indonesia consists of three divisions, namely Quality Operations (Qops), Quality Document Control & Regulatory Compliance (QDoc), and Quality System (QS). The QDoc division at PT. Abbott Indonesia has important duties and roles, namely document preparation, document storage, document destruction, and checking the effectiveness of documents distributed to each area. Change control is a system used to assess/review and control changes that affect materials and processes that have been registered/listed in accordance with Good Manufacturing Practice (GMP) & Good Distribution Practice (GDP). Regulatory Compliance is responsible for preparing documents related to product registration to be submitted to the Regulatory Body (local and export country). Conclusion: PT. Abbott Indonesia has implemented CPOB aspects well in every aspect and series of its production processes.